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Tulisokibart

Alternative Names: Tulisokibart, MK-7240, PRA-023, MK7240, PRA023, PRA 023, PRA023-Companion-diagnostic
Latest Update: 2024-05-09
Latest Update Note: News Article

Product Description

PRA023, is a monoclonal antibody against cytokine TL1A, a target associated with both intestinal inflammation and fibrosis. (Sourced from: https://prometheusbiosciences.com/pipeline/pra023/)

Mechanisms of Action: TL1A Antagonist

Novel Mechanism: Yes

Modality: Antibody

Route of Administration: Intravenous,Subcutaneous

FDA Designation: None *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: Merck
Company Location: KENILWORTH NJ 07033
Company CEO: Robert M. Davis
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Tulisokibart

Countries in Clinic: Australia, Belgium, Canada, Czech Republic, France, Georgia, Germany, Hungary, Israel, Italy, Netherlands, Norway, Poland, Spain, Switzerland, United Kingdom, United States

Active Clinical Trial Count: 9

Highest Development Phases

Phase 3: Colitis, Ulcerative

Phase 2: Crohn Disease|Lung Diseases, Interstitial|Scleroderma, Diffuse|Scleroderma, General|Scleroderma, Systemic

Phase 1: Healthy Volunteers

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

MK-7240-001

P3

Recruiting

Colitis, Ulcerative

2026-11-21

33%

ATHENA-SSc-ILD

P2

Recruiting

Scleroderma, Diffuse|Scleroderma, Systemic|Scleroderma, General|Lung Diseases, Interstitial

2025-12-19

46%

2021-000092-37

P2

Active, not recruiting

Crohn Disease

2025-10-14

The ATHENA-SSc-ILD Study.

P2

Active, not recruiting

Scleroderma, General

2025-06-09

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